AQUAPAK 020 HUMIDIFIER ADAPTER

AQUAPAK 020 HUMIDIFIER ADAPTER is an FDA 510(k)-cleared medical device (K833974) manufactured by Respiratory Care, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 15, 1983. Regulation: 8.